Taiwan FDA registration 88dca6e632c597cf872994a242c4ff40

"Lane" Manual Eye Surgery Instruments (Unsterilized)

TW: "萊恩" 手動式眼科手術器械 (未滅菌)

Taiwan·Risk Class 1·RHEIN MEDICAL INC.·Registered May 31, 2011 – May 31, 2016Cancelled

Registration details

Analysis ID: 88dca6e632c597cf872994a242c4ff40
Customs Code: DHA04401042709

Company information

Manufacturer: RHEIN MEDICAL INC.
Manufacturer Country: United States
Authorized Representative: RAY HUNG INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4350 手動式眼科手術器械
Import Information: import

Dates and status

Registration Date: May 31, 2011
Expiry Date: May 31, 2016
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Lane" Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88dca6e632c597cf872994a242c4ff40 and manufactured by RHEIN MEDICAL INC.. The authorized representative in Taiwan is RAY HUNG INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.